Production Engineer
Responsibility: In the Production Engineering department of Roche's Instrument Operation Network (ION), you will design, optimize, and maintain production processes and product designs for medical diagnostic devices. You will manage technical changes, coordinate projects, and support the transfer of new and existing products to commercial production within a GMP environment.
Location
Rotkreuz (ZG), Switzerland
Workload: 100 %
Employment type: Permanent, Immediate start (or from 1 July 2026)
Languages
German – Verbal: very good, Written: very good
English – Verbal: very good, Written: very good
Responsibilities
Coordinate technical changes: plan, coordinate, evaluate, assign tasks, and implement changes in alignment with Product Leaders or Sub‑Chapter Leads.
Create and maintain specifications, test documentation, work plans, master data, and bill-of-materials, and ensure smooth input and output control of changes in production.
Proactively monitor and communicate to ensure timely completion of Engineering Change Requests (ECRs).
Ensure compliance with quality goals, deadlines, and regulatory requirements, including responsibility for test documentation and master data for product manufacturing.
Manage small projects assigned by Product Lead or Sub‑Chapter Lead, such as continuous improvement and harmonization projects.
Aid in development projects, support creation of samples and prototypes, coordinate required materials, and provide feedback on manufacturability.
Qualifications
Completed technical education (FH or state‑certified technician) in technology and automation engineering.
Minimum 5 years of professional experience in assembly, testing, claim handling, and repair of medical diagnostic devices. Practical experience in device assembly or electronic technical roles is advantageous.
Experience in transferring new projects to production, designing production lines, managing material data, and building and repairing breadboards and functional prototypes of complex mechatronic systems in a GMP environment, preferably for regulated medical devices.
Demonstrated ability to coordinate complex processes, manage change and stakeholders, and actively improve existing structures with a service mindset and proactive attitude.
Strong teamwork and communication skills for effective work in an international matrix organization. Very good German and English language skills (spoken and written) are essential for collaboration across Germany, Switzerland, and the USA.
Willingness to learn new digital tools, flexibility, and a sense of responsibility in a changing environment.
Occasional travel to neighboring countries is acceptable.
Nice to Have
Knowledge of SAP
Additional Information
Start date: 01 July 2026 (latest possible start date: 01 August 2026)
Job duration: 12 months or more
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